1010800-67-5

Basic information

• Product Name: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate
• Synonyms: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate
• CAS NO: 1010800-67-5
• Molecular Weight: 264.321
• Mol File: 1010800-67-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate(1010800-67-5)
• EPA Substance Registry System: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate(1010800-67-5)

Safety Data

• Hazardous Substances Data: 1010800-67-5(Hazardous Substances Data)

Upstream product

• 1663-39-4 tert-Butyl acrylate 
• 7099-91-4 p-methoxybenzoylformic acid 
• 115-11-7 isobutene 
• 3153-44-4 4-(4-methoxy-phenyl)-4-oxo-butyric acid 

Downstream Products

• 1304688-94-5 (S)-tert-butyl 4-hydroxy-4-(4-methoxyphenyl)butanoate 
• 128994-28-5 (S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 594847-89-9 (S)-1-(4’-methoxyphenyl)butan-1,4-diol 
• 1314858-00-8 (R)-5-(4-methoxyphenyl)pyrrolidin-2-one 
• 1314842-85-7 (S)-5-(4-methoxyphenyl)pyrrolidin-2-one 
• 126135-42-0 (R)-(+)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 1010801-83-8 C₂₈H₂₇F₃N₆O₄ 
• 54851-73-9 6-(4-hydroxyphenyl)-3(2H)-pyridazinone 
• 2166-33-8 6-(4-methoxyphenyl)-2H-pyridazin-3-one 
• 1010801-81-6 C₂₈H₂₉F₃N₆O₄ 
• 39560-33-3 6-(4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone 
• 3153-44-4 4-(4-methoxy-phenyl)-4-oxo-butyric acid 
• 1357377-81-1 tert-butyl 4-(4-methoxyphenyl)-4-(4-methoxyphenylimino)butanoate 
• 1017-06-7 6-(4-Methoxyphenyl)-4,5-dihydro-2H-pyridazin-3-one 

Relevant articles and documents

Acyl radicals from α-keto acids using a carbonyl photocatalyst: Photoredox-catalyzed synthesis of ketones

Acyl radicals have been generated from α-keto acids using inexpensive and commercially available 2-chloro-thioxanthen-9-one as the photoredox catalyst under visible light illumination. These reactive species added to olefins or coupled with aryl halides via a bipyridylstabilized Ni(II) catalyst, enabling easy access to a diverse range of ketones. This reliable, atom-economical, and eco-friendly protocol is compatible with a wide range of functional groups.